VERONIQUE GELARD

Informations personnelles

Nom complet

VERONIQUE GELARD

Genre

Femme

Pays

SWITZERLAND

Canton

Geneve

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Données professionnelles

Fonction

Team Manager-Clinical Trial Management-Project Management-Monitoring

Domaine d'activité

Privé

Statut

Autre

Position

Cadre

Biographie / CV

DAS-Diploma of Advanced Studies in Management of Clinical TrialsHôpitaux Universitaires de Genèveoctobre 2012 – Aujourd'hui (10 mois)Région de Genève, SuisseAcquisition of the theoretical and practical understanding of how Good Clinical Practice (GCP) principles are shaping each step of a Clinical Trial, including study design, trial management and conduct as well as data management and analysis.Manager of the Customer Service/Medical Information Response CenterLilly Export S.A2005 – janvier 2013 (8 ans)Région de Genève, SuisseExtensive experience of managing people in a demanding customer service. Continuous service improvement and project management.Customer Service CoordinatorEli Lilly Export SAnovembre 2001 – 2004 (3 ans)Région de Genève, SuisseAcquisition of complex scientific content of 2 marketed products in Cardiology and Intensive Care Unit to provide Medical Information responses in English and French to questions from 16 European countries’ Healthcare Professionals.Specialty Services SupervisorCovance CLSmai 1998 – octobre 2001 (3 ans 6 mois)Région de Genève, SuisseImplementation and development of the Patient Information Monitoring Services department within the Geneva office in collaboration with our US headquarter. Management of a team of 5 persons.Senior Assistant in Quality Assurance Department mars 1994 – avril 1998 (4 ans 2 mois)Région de Genève, SuisseConduct of internal audits in the laboratory (CAP accreditation); Writing audits reports and follow up for corrective actions.Participation in sponsor’s audit; responsible for lab data archives and SOPs documentation.Technician and Chief Technician for Pulmonary/Pharmacology/Asthma Research UnitRCC1986 – 1994 (8 ans)Région de Genève, SuisseSet up of the entire laboratory in collaboration with the company headquarter.Responsible for the entire testings’ schedule: from animal orders till the final data analysis.FormationUniversity of GenevaDAS Certificate of Advanced Studies in Management of Clinical Trials, Clinical Trials - Good Clinical Practice- Quality Processes2012 – 2013Ecole La Martinière LyonBachelor Lab. tech, Biologie1972 – 1975

Activité

Finalizing the DAS- Diploma of Advanced Studies in Management of Clinical Trials– GCP Implementation and Quality Processes, aimed for key players like Clinical Research Associates (CRA), Clinical Research Scientists (CRS), Data Managers (DM), Clinical Research Coordinators (CRC), Clinical Trial Managers (CTM) and regulatory affairs specialists.

Compétences

Medical professionalExtensive experience in the clinical laboratory and clinical research.Quality Assurance and Monitoring Within a global Contract Research Organization, conduct of internal audits; SOPs maintenance.Implementation and development of the Patient Information Monitoring Services department.People Manager Of a call Center/ Customer Service, providing Medical Information for marketed drugs in Europe in Cardiology and Intensive Care Units within a Global Pharmaceutical Company.Project ManagementActive participation in local and regional projects to develop new servicesSubject Matter Expert in a regional project; Transition Leader role#Français-Anglais

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